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Visit the WebMD Parkinson's Health Center for information about symptoms, types, diagnosis, treatment and care.

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Love and peace

I am a 59 year old male with 10 years of PD. My Neurologist talked to me about DBS in the future. The...

Posted by Anon_229944

0 Replies | Reply | Watch This Discussion Report This | Share this:Love and peace I am a 59 year old male with 10 years of PD. My Neurologist talked to me about DBS in the future. The...

Parkinson's related to toxics exposure

My husband was recently diagnosed with Parkinson's. Some materials we have read indicate Parkinson's may be...

Posted by Anon_48692

1 Reply | Reply | Watch This Discussion Report This | Share this:Parkinson's related to toxics exposure My husband was recently diagnosed with Parkinson's. Some materials we have read indicate Parkinson's may be...

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CO-Q10

Has anyone tried this,I saw that there were some on going studies going on and saw some help with balance and...

Posted by lepman

1 Reply | Reply | Watch This Discussion Report This | Share this:CO-Q10 Has anyone tried this,I saw that there were some on going studies going on and saw some help with balance and...

Parkinson's and Extreme Fatigue

I am 47 and diagnosed with early stage Parkinson's last spring. Slight tremor right hand, internal tremor,...

Posted by marymc0903

7 Replies | Reply | Watch This Discussion Report This | Share this:Parkinson's and Extreme Fatigue I am 47 and diagnosed with early stage Parkinson's last spring. Slight tremor right hand, internal tremor,...

C-pap Machine and sleep apneaha

Lately I have been wakeing up during the night caughing and chokeing in my sleep, a few times vommiting because...

Posted by lepman

0 Replies | Reply | Watch This Discussion Report This | Share this:C-pap Machine and sleep apneaha Lately I have been wakeing up during the night caughing and chokeing in my sleep, a few times vommiting because...

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azilect and tyramine

Dr. Stacy: Is it true that tyramine rich foods are not as dangerous as once thought when taking a maoi? I was...

Posted by An_248640

1 Reply | Reply | Watch This Discussion Report This | Share this:azilect and tyramine Dr. Stacy: Is it true that tyramine rich foods are not as dangerous as once thought when taking a maoi? I was...

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Vision problems

I am noticing that I am having significant problems with my eyes when I shift from reading or doing close...

Posted by lovedogs1955

32 Replies | Reply | Watch This Discussion Report This | Share this:Vision problems I am noticing that I am having significant problems with my eyes when I shift from reading or doing close...

Newly diagnosed Parkinson's Disease Patient Scared...

I am a 58 year old female who was recently diagnosed with PD and am scared to death of what is going to...

Posted by Ktowngirl

2 Replies | Reply | Watch This Discussion Report This | Share this:Newly diagnosed Parkinson's Disease Patient Scared to Death I am a 58 year old female who was recently diagnosed with PD and am scared to death of what is going to...

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PD symptoms or Infection

How lucky am I to find Dr. Stacy on WebMD?!? My mother was a patient of yours up until 3 yrs ago when we...

Posted by An_250062

How lucky am I to find Dr. Stacy on WebMD?!? My mother was a patient of yours up until 3 yrs ago when we moved to the West Coast and I brought her with me. About that time she developed her first UTI which you diagnosed via email. Her only symptoms were confusion, hallucinations, and very sudden and sporadic slurred speech and loss of movement. She has had frequent UTI's ever since and the urologists seem to be at a loss. I understand these are common in PD patients. Each time she gets one my first clues are the hallucinations and confusion. For the past 6 mos they have been constant. She tests positive for UTI, receives oral antibiotics and then about a week after the treatment finishes we're back to square one. I have suggested to both the PCP and the urologist that perhaps she has never been cured of the infection and needs a stronger injection or IV antibiotic. One told me they would not hospitalize for UTI and another told me I'd have to take her to the ER to get her admitted. Well I tried that on two occasions but since the dipstick tested negative at the time (probably due to the recent completion of oral antiobiotics) they would not admit her. I think both of these doctors as well as several caregivers believe this is just end-of-life PD. I've also been told that even though her cultures grow positive for E-coli bacteria anyone's urine would do so after the allotted time so maybe she doesn't even have an infection. ?? After reading several posts online it does sound like this is how the last few days of a PD patient's life can be described. When I read these posts I have to wonder was it really end of life for these patients or were they possibly infected with bacteria that might have made them seem off kilter. I've really struggling with this right now. Everyone is beginning to make me feel like I am the crazy one and that I cannot accept the fact my mother is dying. If it is end of life PD I can accept that and I hope her suffering ends quickly. But I don't know how to be sure whether it is that or the infection. Your advise is greatly appreciated!View Thread

Posted byAn_250062

1 Reply | Reply | Watch This Discussion Report This | Share this:PD symptoms or Infection How lucky am I to find Dr. Stacy on WebMD?!? My mother was a patient of yours up until 3 yrs ago when we...

PD Symptoms vs Infection

How lucky am I to find Dr. Stacy on WebMD?!? My mother was a patient of yours up until 3 yrs ago when we...

Posted by An_250062

How lucky am I to find Dr. Stacy on WebMD?!? My mother was a patient of yours up until 3 yrs ago when we moved to the West Coast and I brought her with me. About that time she developed her first UTI which you diagnosed via email. Her only symptoms were confusion, hallucinations, and very sudden and sporadic slurred speech and lose of movement. She has had frequent UTI's ever since and the urologists seem to be at a loss. I understand these are common in PD patients. Each time she gets one my first clues are the hallucinations and confusion. For the past 6 mos they have been constant. She tests positive for UTI, received oral antibiotics and then about a week after the treatment finishes we're back to square one. I have suggested to both the PCP and the urologist that perhaps she has never been cured of the infection and needs a stronger injection or IV antibiotic. One told me they would not hospitalize for UTI and another told me I'd have to take her to the ER to get her admitted. Well I tried that on two occasions but since the dipstick tested negative at the time (probably due to the recent completion of oral antiobiotics) they would not admit her. I think both of these doctors as well as several caregivers believe this is just end-of-life PD. After reading several posts online it does sound like this is how the last few days of a PD patient's life can be described. When I read these posts I have to wonder was it really end of life for these patients or were they possibly infected with bacteria that might have made them seem off kilter. I've really struggling with this right now. Everyone is beginning to make me feel like I am the crazy one and that I cannot accept the fact my mother is dying. If it is end of life PD I can accept that and I hope her suffering ends quickly. But I don't know how to be sure whether it is that or the infection. Your advise is greatly appreciated!View Thread

Posted byAn_250062

0 Replies | Reply | Watch This Discussion Report This | Share this:PD Symptoms vs Infection How lucky am I to find Dr. Stacy on WebMD?!? My mother was a patient of yours up until 3 yrs ago when we...

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diagnosis of parkinsons

I was diagnosed with parkinsons about 2 years ago,at the time I went to the doctor I had several problems one...

Posted by cheney13

3 Replies | Reply | Watch This Discussion Report This | Share this:diagnosis of parkinsons I was diagnosed with parkinsons about 2 years ago,at the time I went to the doctor I had several problems one...

Over medicated!

I was just release from the hospital about 2 weeks ago from being over medicated. I have three doctors and...

Posted by Sandee54

0 Replies | Reply | Watch This Discussion Report This | Share this:Over medicated! I was just release from the hospital about 2 weeks ago from being over medicated. I have three doctors and...

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Azilect/Sinemet in elderly and interactions with a...

My mother (75 year-old, osteoarthritis, depression) was diagnosed with PD one month ago. I was worried about...

Posted by Milmanda

My mother (75 year-old, osteoarthritis, depression) was diagnosed with PD one month ago. I was worried about slowliness, confusion and lack of concentration and, suspecting dementia, led her to a neurologist. To my surprise, after a very brief evaluation, the doctor saw it clear: mild PD, predominantly in the right side. He prescribed Azilect, as he found her functional state to be fairly good, and Azilect could be neuroprotective, slowing PD progression.

Azilect seemed to be attractive, but I read about it, and I saw contradictory information about neuroprotection, and, importantly, about interactions with antidepressants. My mother has been on escitalopram 15 and mirtazapine for three years (maybe three years with non-diagnosed PD).

So, I seeked a second opinion. We live in Santiago de Compostela, Spain, and it is not easy to find highly specialized doctors, but I had the luck to get an appointment with the chief of the Unit of Movement Disorders in our University Hospital. Afther a more thorough examination, this second doctor confirmed mild PD, but did not recommend Azilect at all. He said Azilect is not the best option for elderly and, specially, he said that interactions with antidepressants could be severe. So, he put my mother on Sinemet Plus (25/100): 1/2, 1, 1/2, slowly introduced, with the aim of having a 1-1-1 protocol.

Some weeks ago, Mum started Sinemet and she seems to have some good effects (balance, stiffness), but I am a bit surprised to see more tremor and eye fasciculations, which I do not know if could be attributed to Sinemet.

And my worst worry is if Sinemet is really the best option. I know of its medium-long-term effects, and I would like to delay its use... But, at the same time, I do not want to prevent my mother to have good quality of life (I do actually think that PD was limiting her life a lot).

So I would like to ask you about the options Azilect/Sinemet. To your knowledge, or in your experience, does it make sense to start Sinemet in an old person, even if her symptoms are not very severe? Would it Azilect a better option? any insights about risks of interactions with antidepressants?

I do not even know if we could cut Sinemet Plus now, but I have conflicting feelings about this otherwise miracle drug.

Please, excuse for this long post. But I feel insecure with my English and want you to understand our situation.

I am stressed, worried and shocked, but happy to have found you.

Thank you very much in advance!View Thread

Posted by Milmanda

2 Replies | Reply | Watch This Discussion Report This | Share this:Azilect/Sinemet in elderly and interactions with antidepressants My mother (75 year-old, osteoarthritis, depression) was diagnosed with PD one month ago. I was worried about...

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Internal Tremor

I was diagnosed with PD over 2 years ago. I rarely have a visible tremor, but I experience an internal,...

Posted by blessijr

2 Replies | Reply | Watch This Discussion Report This | Share this:Internal Tremor I was diagnosed with PD over 2 years ago. I rarely have a visible tremor, but I experience an internal,...

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Dopamine Dysregulation Syndrome

I have written about this subject before,but I have'nt seen much new on this site or any others. Dopamine...

Posted by sparky1109

2 Replies | Reply | Watch This Discussion Report This | Share this:Dopamine Dysregulation Syndrome I have written about this subject before,but I have'nt seen much new on this site or any others. Dopamine...

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parkinson related illness

my husband has parkinson, so far just on the right side. I have heard that there are other illness related to...

Posted by An_249641

2 Replies | Reply | Watch This Discussion Report This | Share this:parkinson related illness my husband has parkinson, so far just on the right side. I have heard that there are other illness related to...

Painful Legs and Moving Toes Syndrome

I was recently diagnosed with PLMT, which is a disorder quite separate and distinct from Parkinson's. However,...

Posted by kmaze001

1 Reply | Reply | Watch This Discussion Report This | Share this:Painful Legs and Moving Toes Syndrome I was recently diagnosed with PLMT, which is a disorder quite separate and distinct from Parkinson's. However,...

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parkinsons and rbd

I would be curious to know how many Parkinson's patients have had REM sleep behavior disease (RBD) before...

Posted by An_249572

6 Replies | Reply | Watch This Discussion Report This | Share this:parkinsons and rbd I would be curious to know how many Parkinson's patients have had REM sleep behavior disease (RBD) before...

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Teling family members I am too tired to cope with ...

My husband and I have a blended family of 8 kids and 21 grandchildren,Wonderful, fun and totally exhausting....

Posted by newshen

7 Replies | Reply | Watch This Discussion Report This | Share this:Teling family members I am too tired to cope with extended stays and extra houseguests. My husband and I have a blended family of 8 kids and 21 grandchildren,Wonderful, fun and totally exhausting....

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Question about sufficiency of medical treatment

Hello, I am a 61-year-old man who was diagnosed with Parkinson's Disease one year ago with first degree...

Posted by mirage_sager

1 Reply | Reply | Watch This Discussion Report This | Share this:Question about sufficiency of medical treatment Hello, I am a 61-year-old man who was diagnosed with Parkinson's Disease one year ago with first degree...

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rigidity

what can be done about RIGIDITY in parkinsons?

Posted by xxxyyyzzz

2 Replies | Reply | Watch This Discussion Report This | Share this:rigidity what can be done about RIGIDITY in parkinsons?

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Is there such a thing as a Parkinson's Flare?

Well, once again I have had an episode that no one seems to understand what happened. When my PD first...

Posted by lovedogs1955

Well, once again I have had an episode that no one seems to understand what happened. When my PD first showed its head to me, it seemed to affect my diaphragm/respiratory muscles first. This lead to severe chest pain and shortness of breath with even minimal activity, including talking/laughing. Over the past 6 years, I have been able to improve in that area, but the same type of pain is now in all of my major muscles and increases with too much activity or stress. That being said, here is what happened a few days ago,

I had one of my two dogs attacked by a larger dog, while my dogs were leashed. The dog that was attacked managed to wiggle out of his harness and took off running. I was afraid for that dog's safety, so I took off after him as fast as I could with my leashed dog and my cane. ( I also wear a leg brace due to foot drop). Long story short, both dogs did fine and we arrived back home in one piece. However, I had a significant amount of chest pain and shortness of breath, which gradually subsided with time and rest, The following afternoon, I was sitting in recliner and watching TV when out of the blue, I had SEVERE chest pain start mid-chest and it "bloomed" upwards going all the way to the top of my head. No nausea or vomiting. No pain down either arm, The pain did not fluctuate...stayed at the same intensity for about 20 minutes. It subsided on its own, but ever since, I am having symptoms like I had when all of this PD started. My husband said that after the episode, my face was pale and my eyes were droopy.

I have spoken with my cardiologist and was seen by my oncologist yesterday. Both of them feel that it was my Parkinson's that was aggrevated by the spurt of running that I did chasing the dog.

I guess my question is this...how would I describe this episode to health care professionals other than "chest pain and shortness of breath?" Is there such a phenomomen as Parkinson's "flare" or "crisis?"View Thread

Posted by lovedogs1955

7 Replies | Reply | Watch This Discussion Report This | Share this:Is there such a thing as a Parkinson's Flare? Well, once again I have had an episode that no one seems to understand what happened. When my PD first...

Painful Legs and Moving Toes

For anyone who may have this condition, I have started a new user community on WebMD. I did see some old posts...

Posted by kmaze001

0 Replies | Reply | Watch This Discussion Report This | Share this:Painful Legs and Moving Toes For anyone who may have this condition, I have started a new user community on WebMD. I did see some old posts...

Head trauma and Parkinson's

My husband was diagnosed with PD in May of 2009. At the time, the only symptom he had was a tremor in his...

Posted by An_249365

0 Replies | Reply | Watch This Discussion Report This | Share this:Head trauma and Parkinson's My husband was diagnosed with PD in May of 2009. At the time, the only symptom he had was a tremor in his...

Can you have two?

I was wondering If a person could have two conditions going on at the same time Like a Neurological and...

Posted by lepman

0 Replies | Reply | Watch This Discussion Report This | Share this:Can you have two? I was wondering If a person could have two conditions going on at the same time Like a Neurological and...

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How to cure her Parkinson's disease?

Today saw the Parkinson's disease, she this year 63 years old, sick 4 years, in Beijing, China and zhengzhou...

Posted by ZUOLEI

1 Reply | Reply | Watch This Discussion Report This | Share this:How to cure her Parkinson's disease? Today saw the Parkinson's disease, she this year 63 years old, sick 4 years, in Beijing, China and zhengzhou...

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why is it.....

Why is it after three years of testing and no answers from the doc's, that when ever you try to describe...

Posted by Anon_157363

Why is it after three years of testing and no answers from the doc's, that when ever you try to describe your fuzzy brain issues you get told right away that your depressed or stressed.And prescribe a medication that just makes you mor dizzy than you alrady feel. I tell them I'm alresdy very dizzy 24/7 and this will make it better? I jump through the hoops and take it just to give it a shot and yep dizzy ten fold even throwing up now. I call them to tell them as to whats going on and they take me off the med. Then upon seeing them again I get told I'm depressed again and stressed so again they give me another drug and yep dizzy ten fold again and yep the vommiting starts up and I call again and get taken off the drug again.

Even after three years of testing and I've asked the docs what tests have'nt I had and got told just about every test was given to you. And I ask and you can't find out what this is or even tell me what was checked for or what has been ruled out? Not even a clue as to whats wrong? after three years?Oh I get told you must be stressed and depressed and give me another med. and once again dizzy ten fold and again get taken off the med.I mean whats going on here, Is it standard practice just to dissmiss your symptoms as just Depression and stress.This merry goround just has to be why this is not going in the right direction. And yes going through this for this long is stressful maybe even a little depressing. But who wouldn't be. I wish I could just take off my head and trade it with the doc's and say when ya get over the dizzieness and other symptoms, figure it out then we can trade back...Because This isn't all in my head.

I wish it were, I could cope with it alot better if it were.You know whats really bad is these docs can't even agree if it's Neurological or Vestibular and the tests just keep getting repeated and guess what else dose too,,you got it Your depressed and stressed, O.K. Do we Really have to go through all this again? At least they do admitt that something is wrong but come on after three years you'd think they would have some kind of clue as to what's gong on here....Wouldn't ya......or at the very least what direction to go with it anyway....Why can't they just man up or woman up and say hey we just can't figure this out But we can send you to someone with a little more experience why could figure this out....But no back to you must be so stressed over this and depressed...this could explain why you are haveing so many symptoms so here try this med.....
Gee...Thanks Doc.......View Thread

Posted byAnon_157363

1 Reply | Reply | Watch This Discussion Report This | Share this:why is it..... Why is it after three years of testing and no answers from the doc's, that when ever you try to describe...

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sinemet cr

Dr. Stacey: I have been on sinemet cr for about 6 years. I recently noticed that AS SOON AS I SWALLOW IT my...

Posted by EW4567

1 Reply | Reply | Watch This Discussion Report This | Share this:sinemet cr Dr. Stacey: I have been on sinemet cr for about 6 years. I recently noticed that AS SOON AS I SWALLOW IT my...

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Parkinsons or P.S.P.

Is there anyone who can tell me more than what I have found out through the internet about P.S.P and about...

Posted by Anon_157363

Is there anyone who can tell me more than what I have found out through the internet about P.S.P and about testing for this and differentiating between the two.I have tremmors mostly in useing my arms and inside tremors not nery much with resting ones.The thing that started up with me first was unexplained joint pain and went to my gp for that and he found out about my balance problem during his exam.

He thought it maybe Manieres and had me tested for it as well as checking for a stroke or any leasions by means of M.R.I's and CT scans.All showed neg.As time went on My balance and coridination have gotten worse and started haveing problems swollowing food or liquids with out sometimes chokeing, and my vision has gotten blurred and even at times seeing double. And hard to look down or up with out the feeling of being dizzy,and the balance is way worse in doing that as well.

My neck is so sore and stiff that I find myself tilting my head against my shoulder most of the time just to get relief from the pain because my head feels like a gaint weight and trying to find balance all the time my head bobbels alot. My thinking process is so messed up I find it very hard to stay focused and planning, problem solving is very difficult,and short term memory is very bad. Slurred speach and finding the right words that I want to say is very difficult.

I have a constant feeling of cotten mouth and no matter how much I drink water I can never keep it from drying out. I have a lot of other things going wrong but they seem to be related more with the Parkinsons Symptoms like ED and lots of numbness in one leg and mucle and joiunt pain and stiffness. I feel like my movements are in slow motion and even sometimes freezing up. I thought I needed new glasses and saw my optomitrist and he found that one of my pupils is bigger than the other and asked if I could feel it being bigger than the other,I didn't, Hummm something new there.and he believes it to be corrilated to what is going on with me and said my perscription hasen't changed and the blurred vision is also related to what is going on.

All I know is that feeling this way is not normal and something is very wrong and this is progressing very fast. Unlike what I have found out about Parkinsons its self this is not really going in stages but seems to be developing symptoms faster and more agressively than in stages. I know that I maybe jumping the gun and self diagnossing maybe more harm than good but the Doc seems stumped about how this is progressing so fast and the tests are just showing normal for my age he tells me.I know I'm only fifty but I don't think either condition is very discrimitive with how old you are.

I'm just trying to get a grip on what this could be and with doing alot of research on my own It just keeps comming up in my mind Parkinsons or P.S.P. but I'm no Doc. So all I can do is educate myself and try to better prepare myself .....

Am I over stepping my bounds here or am I justified in doing this.....View Thread

Posted byAnon_157363

3 Replies | Reply | Watch This Discussion Report This | Share this:Parkinsons or P.S.P. Is there anyone who can tell me more than what I have found out through the internet about P.S.P and about...

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